113133-46-3

Basic information

• Product Name: 3-(BENZYLOXY)BUTAN-2-ONE
• Synonyms: (R)-3-Benzyloxy-butan-2-one;3-(benzyloxy)butan-2-one;3-benzyloxy-2-butanone
• CAS NO: 113133-46-3
• Molecular Formula: C11H14O2
• Molecular Weight: 178.231
• Mol File: 113133-46-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 3-(BENZYLOXY)BUTAN-2-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(BENZYLOXY)BUTAN-2-ONE(113133-46-3)
• EPA Substance Registry System: 3-(BENZYLOXY)BUTAN-2-ONE(113133-46-3)

Safety Data

• Hazardous Substances Data: 113133-46-3(Hazardous Substances Data)

Upstream product

• 2040-44-0 ethyl 2-benzyloxypropionate 
• 827308-05-4 2-benzyloxy-1-(morpholin-4-yl)-1-propanone 
• 513-86-0 3-hydroxy-2-butanon 
• 100-51-6 benzyl alcohol 
• 53329-00-3 [(but-3-en-2-yloxy)methyl]benzene 
• 20194-18-7 sodium phenyl-methanolate 
• 156093-87-7 (3S)-3-(benzyloxy)-1-chloro-2-butanone 
• 100-39-0 benzyl bromide 
• 23147-57-1 2,5-dihydroxy-2,3,5,6-tetramethyl-1,4-dioxane 
• 115170-84-8 2-(benzyloxy)-3-nitrobutane 

Downstream Products

• 114418-30-3 (2R,3S)-3-(benzyloxy)butan-2-ol 
• 77312-73-3 3-benzyloxybutan-2-ol 
• 124338-53-0 (2S,3R)-3-(benzyloxy)butan-2-ol 
• 110549-55-8 (E)-(4S,5S,6S)-6-Benzyloxy-5-(2-methoxy-ethoxymethoxy)-3,5-dimethyl-hept-2-en-4-ol 
• 110549-54-7 (E)-(4R,5S,6S)-6-Benzyloxy-5-(2-methoxy-ethoxymethoxy)-3,5-dimethyl-hept-2-en-4-ol 
• 107657-73-8 (Z)-(4S,5S,6S)-6-Benzyloxy-5-(2-methoxy-ethoxymethoxy)-3,5-dimethyl-hept-2-en-4-ol 
• 107613-12-7 (Z)-(4R,5S,6S)-6-Benzyloxy-5-(2-methoxy-ethoxymethoxy)-3,5-dimethyl-hept-2-en-4-ol 
• 110510-54-8 (+/-)-(2S^*,3R^*)-3-(benzyloxy)-2-<(2-methoxyethoxy)methoxy>-2-methyl-1-butanal 
• 110510-53-7 (+/-)-(3R^*,4R^*)-4-(benzyloxy)-3-<(2-methoxyethoxy)methoxy>-3-methyl-1-pentene 
• 388066-93-1 (6R,8R)-7,7-dimethyl-2-[1-(phenylmethoxy)ethyl]-5,6,7,8-tetrahydro-6,8-methanoquinoline 
• 108229-25-0 (((3-methylbut-3-en-2-yl)oxy)methyl)benzene 
• 77312-73-3 3-benzyloxy-2-butanol 
• 98095-59-1 (+/-)-(3R^*,4R^*)-4-(benzyloxy)-3-methyl-1-penten-3-ol 

Relevant articles and documents

Acid-catalyzed reaction of 2-hydroxycyclobutanone with benzylic alcohols

The acid-promoted syntheses of 2-(benzyloxy)cyclobutanones and bis(benzyloxy)dioxatricyclo decanes were achieved starting from 2-hydroxycyclobutanone and variously functionalized benzyl alcohols. The reaction sequences afforded the desired products in good to high yields and in a solvent-dependent chemoselective fashion.

Optical resolution of acyclic α-hydroxy ketone derivatives by inclusion complexation

A new method for the preparation of optically active acyclic α-hydroxy ketone derivatives by thermodynamic resolution using a chiral host compound is described. We examined the resolution of racemic 2-benzyloxy-3-pentanone with chiral host compounds in va

Enethiolizable thioacylsilanes as intermediates for the synthesis of thietanols, thiolanols, and thianols

Thietanols, thiolanols, and thianols (tetrahydro-2H-thiopyran-3-ols) can be obtained by a fluoride-mediated cyclization of (Z)-α-silyl vinyl sulfides containing an ω-carbonyl function in the chain bonded to the sulfur.